biochemical model of C 3 photosynthesis ( Farquhar et al., 1980 ) to estimate the conductance of CO 2 from the intercellular air spaces to the site of carboxylation inside the chloroplast. This method has been found to compare well with other methods ( Bunce
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Soo-Hyung Kim and Bert Cregg
Katherine F. Garland, Stephanie E. Burnett, Michael E. Day, and Marc W. van Iersel
increased sensitivity of stomata to abscisic acid, the primary hormone responsible for stomatal closure during water stress ( Pospíšilová and Dodd, 2005 ). Even non-stomatal limitations to photosynthesis such as the maximum carboxylation rate of rubisco (Vc
Juan Carlos Díaz-Pérez
., Ramsey, NJ). Leaf gas exchange and photosystem II efficiency. Simultaneous measurements of leaf gas exchange (net photosynthesis, g S , transpiration, and internal CO 2 concentration) and fluorescence determined as photosystem II (PSII) efficiency were
Giverson Mupambi, Stefano Musacchi, Sara Serra, Lee A. Kalcsits, Desmond R. Layne, and Tory Schmidt
( Murata et al., 2007 ). The measurement of photosynthetic light use efficiency can be used to estimate plant photosynthesis and net primary production ( Flanagan et al., 2015 ; Liu et al., 2013 ). Leaf-level photosynthetic light use efficiency can be
Lie Li, Yu-xin Tong, Jun-ling Lu, Yang-mei Li, and Qi-chang Yang
proportional stage of the CO 2 photosynthetic curve was fitted to Rubisco activity (carboxylation efficiency), whereas the maximum net photosynthetic rate was fitted to P m . Observations of stomata. To perform stomata observations, rubber elastic impression
Donavon Sonnenberg, Patrick A. Ndakidemi, Ambrose Okem, and Charles Laubscher
by improving the photosynthetic efficiency of plants. Plant biomass production is directly dependent on the net photosynthetic rate ( Sing et al., 2013 ). Photosynthesis is the process by which photosynthetically active radiation (within the
Amanda J. Taylor, R. Thomas Fernandez, Pascal Nzokou, and Bert Cregg
carboxylation capacity resulting from reduced foliar N at high irrigation rates was not a factor affecting Δ 13 C of trees. Thus, we speculate that g wv must be limiting assimilation of 13 C into plant tissue. Water use efficiency based on gas exchange
Soohyun Kang, Yating Zhang, Yuqi Zhang, Jie Zou, Qichang Yang, and Tao Li
photosynthesis rates ( A n ) to ( A ) photosynthetic photon flux density ( PPFD ) and ( B ) intercellular CO 2 partial pressures ( C i ), as well as the quantum efficiency of photosynthetic system II (ΦPSII) to ( C ) PPFD and ( D ) C i . Error bars show ± se
Alefsi David Sánchez-Reinoso, Gustavo Adolfo Ligarreto-Moreno, and Hermann Restrepo-Díaz
efficiency ( iWUE ) was also calculated as a product of the relationship between photosynthesis and g S . Carboxylation efficiency was calculated by the ratio of photosynthesis and intercellular CO 2 concentration ( P n /C i ). Gas exchange measurements
Vahid Rahimi Eichi, Stephen D. Tyerman, and Michelle G. Wirthensohn
Mesophyll conductance to CO 2 in Arabidopsis thaliana New Phytol. 175 501 511 Garland, K.F. Burnett, S.E. Day, M.E. Van Iersel, M.W. 2012 Influence of substrate water content and daily light integral on photosynthesis, water use efficiency, and morphology